Myopia 27, Autosomal Dominant (MYP27)

Alias:
Myopia 27
Myp27
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myopia 27, Autosomal Dominant, is also known as myopia 27. An important gene associated with Myopia 27, Autosomal Dominant is CPSF1 (Cleavage And Polyadenylation Specific Factor 1). Affiliated tissues include retina and eye, and related phenotypes are increased axial length of the globe and high myopia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
4
1

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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